HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600622Generated: October 30, 2026
2-Amino-5-nitropyridine → HCID 67273481, compound
https://huagongshe.com/reaction/600622
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-5-nitropyridine | HCID 77888 | — |
| Reactant | 3-Bromo-1-phenylpropane-1,2-dione | HCID 12568911 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67273481 | HCID 67273481 | 87.5% |
Reaction Steps
To a solution of 0.48 g of 3-bromo-1-phenylpropane-1,2-dione in a mixture of 3 mL of THF and 0.5 mL of ethanol is added 0.25 g of 2-amino-5-nitropyridine. The reaction mixture is heated for 15 minutes at 160° C. in a microwave machine. The solid formed is separated out, taken up in 3 mL of ethanol and refluxed for 6 hours. After evaporating off the solvent, the residue is taken up in ethyl acetate and diluted with sodium hydroxide solution. The organic phase is washed with water, dried and then evaporated to give 0.42 g of (6-nitroimidazo[1,2-a]pyridin-2-yl)(phenyl)methanone in the form of a brown solid, which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902219B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-f68d61f29edf4a5db764361f4214abe6 |
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| Source note | uspto-grants-2011_03 |
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